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4-(Trifluoromethyl)aniline → HCID 69201865、化合物

HRID 898825
ノート
印刷プレビュー

反応式

HRID 898825 の反応式
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1.[C:12]([N:18]1[CH2:22][CH2:21][O:20][C:19]1=[O:23])(=[O:17])[CH:13]=[CH:14][CH2:15][CH3:16].[Cl-].[NH4+]>C1(C)C=CC=CC=1>[F:1][C:2]([F:10])([F:11])[C:3]1[CH:9]=[CH:8][C:6]([NH:7][CH:14]([CH2:15][CH3:16])[CH2:13][C:12]([N:18]2[CH2:22][CH2:21][O:20][C:19]2=[O:23])=[O:17])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 99644-(Trifluoromethyl)anilineHCID 25517Ammonium ChlorideHCID 69200777HCID 69200777、化合物

生成物 1

HCID 69201865HCID 69201865、化合物収率 50%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution of 4-trifluoromethylaniline (193 mg, 1.2 mmol) and 3-(2-pentenoyl)-1,3-oxazolidin-2-one (189 mg, 1.0 mmol) in toluene (3 ml) in a stream of nitrogen was added Pd((R)-binap)(H2O)2(OTf)2 (26.6 mg, 0.025 mmol), and the resulting mixture was stirred at room temperature for 16 hours. After completion of the reaction, a saturated aqueous solution of ammonium chloride (10 ml) was added to the reaction mixture and the mixture was extracted with ethyl acetate (10 ml). The organic layer was dried over anhydrous magnesium sulfate. The solvent was then evaporated off and the crude product obtained was purified by a silica gel column chromatography (hexane:ethyl acetate=1:1) to give the objective compound 3-[3-(4-trifluoromethylanilino)pentanoyl]-1,3-oxazolidin-2-one (165 mg, 50% yield). Enantiomeric excess ratio of this product was determined by a liquid chromatography using a column for separation of optical isomers (column: OA-2000) to be 70% e.e.

後処理

  1. customAfter completion of the reaction
  2. extractionthe mixture was extracted with ethyl acetate (10 ml)
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. customThe solvent was then evaporated off
  5. customthe crude product obtained
  6. customwas purified by a silica gel column chromatography (hexane:ethyl acetate=1:1)

出典と根拠

ORDレコード
ord-fdc4f6473c26412cbf136a15dc8244f1
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07351849B2

反応ノート

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